CREST PRO-HEALTH FOR ME ANTICAVITY FLUORIDE- sodium fluoride rinse 
The Procter & Gamble Manufacturing Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Crest ® Pro-Health For Me™

Anticavity Fluoride Rinse

Drug Facts

Active ingredient

Sodium Fluoride 0.022% (0.01% w/v fluoride ion)

Purpose

Anticavity

Use

Aids in the prevention of dental cavities

Warnings

Keep out of reach of children. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Adults and children 6 years & older: Use twice a day after brushing your teeth with a toothpaste.
  • To dispense 10 mL dose: Remove cap and squeeze the front and back of the bottle (not the sides) to fill the reservoir. Allow excess liquid to drain back into the bottle. Pour out the dose.
  • Vigorously swish the 10 mL of rinse between your teeth for 1 minute and then spit out.
  • Do not swallow the rinse.
  • Do not eat or drink for 30 minutes after rinsing.
  • Instruct children under 12 years of age in good rinsing habits (to minimize swallowing).
  • Supervise children as necessary until capable of using without supervision.
  • Children under 6 years of age: Consult a dentist or doctor.

Inactive ingredients

water, glycerin, propylene glycol, poloxamer, polysorbate 80, phosphoric acid, sodium benzoate, potassium sorbate, flavor, sodium saccharin, disodium phosphate, green 3.

Questions?

1-800-285-9139

DISTR. BY
PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 500 mL Bottle Label

ALCOHOL FREE
BREEZY MINT

DiSNEY
MAGIC TIMER™

STAR
WARS

Crest®
PRO-HEALTH
FOR ME

ANTICAVITY FLUORIDE RINSE

IMPORTANT: READ DIRECTIONS FOR PROPER USE
FIGHTS CAVITIES

ADA
Accepted
American
Dental
Association ®

500 mL (16.9 FL OZ)

96987154

PRINCIPAL DISPLAY PANEL - 500 mL Bottle Label
CREST PRO-HEALTH FOR ME  ANTICAVITY FLUORIDE
sodium fluoride rinse
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-006
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
PHOSPHORIC ACID (UNII: E4GA8884NN)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
Product Characteristics
ColorturquoiseScore    
ShapeSize
FlavorWINTERGREENImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37000-006-15500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/19/201504/10/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35501/19/201504/10/2023
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 4/2023
 
The Procter & Gamble Manufacturing Company